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69541-62-4

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69541-62-4 Usage

General Description

BOC-D-TYR(2,6-DI-CL-BZL)-OH is a chemical compound used in the field of biochemistry and pharmaceuticals. It is a derivative of the amino acid tyrosine, with BOC-D-TYR representing the amino acid with a protective BOC (tert-butyloxycarbonyl) group attached to it. The compound also contains 2,6-DI-CL-BZL, which stands for 2,6-dichlorobenzoyl, an additional protective group. BOC-D-TYR(2,6-DI-CL-BZL)-OH is used in the synthesis of peptide chains and has applications in drug development, particularly for the creation of peptide-based pharmaceuticals. It is also used in research and development to study the structure and function of proteins and peptides. Overall, BOC-D-TYR(2,6-DI-CL-BZL)-OH plays a crucial role in the advancement of biochemistry and pharmaceutical sciences.

Check Digit Verification of cas no

The CAS Registry Mumber 69541-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,5,4 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69541-62:
(7*6)+(6*9)+(5*5)+(4*4)+(3*1)+(2*6)+(1*2)=154
154 % 10 = 4
So 69541-62-4 is a valid CAS Registry Number.

69541-62-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-D-TYR(2,6-DI-CL-BZL)-OH

1.2 Other means of identification

Product number -
Other names T-BUTYLOXYCARBONYL-O-2,6-DICHLOROBENZYL-D-TYROSINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69541-62-4 SDS

69541-62-4Relevant articles and documents

Synthesis and biological activity of N-substituted aminocarbonyl-1,3- dioxolanes as VLA-4 antagonists

Rehman, Abdul,Soni, Ajay,Naik, Keshav,Nair, Sreeji,Palle, Venkata P.,Dastidar, Sunanda,Ray, Abhijit,Alam,Salman, Mohammad,Cliffe, Ian A.,Sattigeri, Viswajanani

scheme or table, p. 5514 - 5520 (2011/01/12)

A novel set of compounds with a 1,3-dioxolane ring which acts as a proline bioisostere have been successfully designed as VLA-4 receptor antagonists. Compounds (18e), (28j), and (35g) were shown to have high receptor affinities.

tert-butoxycarbonylation of amino acids and their derivatives: N-tert-butoxycarbonyl-L-phenylalanine

Keller, Oskar,Keller, Walter E.,Van Look, Gert,Wersin, Gernot

, p. 160 - 160 (2017/06/01)

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